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3. Qaulity-control plan for intravenous admixture programs. II: Validation of operator technique. Morris BG; Avis KE; Bowles GC Am J Hosp Pharm; 1980 May; 37(5):668-72. PubMed ID: 7386475 [TBL] [Abstract][Full Text] [Related]
4. I.V. admixture contamination rates: traditional practice site versus a class 1000 cleanroom. Thomas M; Sanborn MD; Couldry R Am J Health Syst Pharm; 2005 Nov; 62(22):2386-92. PubMed ID: 16278330 [TBL] [Abstract][Full Text] [Related]
5. Method for testing aseptic technique of intravenous admixture personnel. Dirks I; Smith FM; Furtado D; White SJ; Godwin HN Am J Hosp Pharm; 1982 Mar; 39(3):457-9. PubMed ID: 7041641 [TBL] [Abstract][Full Text] [Related]
6. Compounding times and contamination rates associated with the preparation of intravenous admixtures in three types of plastic containers. Allinson RR; Stach PE; Sherrin TP; Latiolais CJ Am J Hosp Pharm; 1979 Apr; 36(4):513-7. PubMed ID: 433938 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of two sterility testing methods for intravenous admixtures. Condella F; Eichelberger K; Foote LC; Griffin RE Hosp Pharm; 1980 Jun; 15(6):305-10. PubMed ID: 10247270 [TBL] [Abstract][Full Text] [Related]
8. Effect of two work practice changes on the microbial contamination rates of pharmacy-compounded sterile preparations. Trissel LA; Gentempo JA; Saenz LM; Woodard MY; Angeles CH Am J Health Syst Pharm; 2007 Apr; 64(8):837-41. PubMed ID: 17420200 [TBL] [Abstract][Full Text] [Related]
9. A first-phase quality assurance program for intravenous admixture aseptic technique. Gurwich EL; Hanold L; Schaeffer P Hosp Pharm; 1982 Mar; 17(3):119-21. PubMed ID: 10255637 [TBL] [Abstract][Full Text] [Related]
10. Premixed intravenous admixtures: a positive development for hospital pharmacy. Lee HE Am J Hosp Pharm; 1983 Jun; 40(6):1043-4. PubMed ID: 6869393 [TBL] [Abstract][Full Text] [Related]
11. Basics of Sterile Compounding: Personnel Requirements for Sterile Compounding. Akers MJ Int J Pharm Compd; 2016; 20(4):307-314. PubMed ID: 28333676 [TBL] [Abstract][Full Text] [Related]
12. Personnel time and preparation costs for compounded versus premixed intravenous admixtures in three community hospitals. Kirschenbaum BE; Cacace L; Anderson RJ; Ackerman LA Am J Hosp Pharm; 1988 Mar; 45(3):605-8. PubMed ID: 3369464 [TBL] [Abstract][Full Text] [Related]
13. Recommended methods for compounding intravenous admixtures in hospitals. Am J Hosp Pharm; 1975 Mar; 32(3):261-70. PubMed ID: 1136973 [TBL] [Abstract][Full Text] [Related]
14. Using a medium-fill simulation to evaluate the microbial contamination rate for USP medium-risk-level compounding. Trissel LA; Gentempo JA; Anderson RW; Lajeunesse JD Am J Health Syst Pharm; 2005 Feb; 62(3):285-8. PubMed ID: 15719586 [TBL] [Abstract][Full Text] [Related]
15. Effect of laminar air flow and clean-room dress on contamination rates of intravenous admixtures. Brier KL; Latiolais CJ; Schneider PJ; Moore TD; Buesching WJ; Wentworth BC Am J Hosp Pharm; 1981 Aug; 38(8):1144-7. PubMed ID: 7270557 [TBL] [Abstract][Full Text] [Related]
16. Control of the aseptic processing environment. Frieben WR Am J Hosp Pharm; 1983 Nov; 40(11):1928-35. PubMed ID: 6650522 [TBL] [Abstract][Full Text] [Related]
17. Sterility-testing program for antibiotics and other intravenous admixtures. Choy FN; Lamy PP; Burkhart VD; Tenney JH Am J Hosp Pharm; 1982 Mar; 39(3):452-6. PubMed ID: 7041640 [No Abstract] [Full Text] [Related]